ClinVar Miner

List of variants studied for Fanconi anemia, complementation group I by Leiden Open Variation Database

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Total variants: 26
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HGVS dbSNP
NM_001113378.2(FANCI):c.1264G>A (p.Gly422Arg) rs146040966
NM_001113378.2(FANCI):c.1264G>C (p.Gly422Arg) rs146040966
NM_001113378.2(FANCI):c.1461T>A (p.Tyr487Ter) rs769248873
NM_001113378.2(FANCI):c.157+78G>A rs963339667
NM_001113378.2(FANCI):c.1583+142C>T rs2053631453
NM_001113378.2(FANCI):c.1840C>T (p.Arg614Ter) rs551399966
NM_001113378.2(FANCI):c.2248T>C (p.Cys750Arg) rs2054124504
NM_001113378.2(FANCI):c.2509G>T (p.Glu837Ter) rs748000458
NM_001113378.2(FANCI):c.2572C>T (p.His858Tyr) rs1361710673
NM_001113378.2(FANCI):c.2T>C (p.Met1Thr) rs2052048258
NM_001113378.2(FANCI):c.3006+3A>G rs1294973649
NM_001113378.2(FANCI):c.3058+1G>A rs149464307
NM_001113378.2(FANCI):c.3058+4A>G rs2054616468
NM_001113378.2(FANCI):c.3350-88A>G rs2054700381
NM_001113378.2(FANCI):c.3437_3455del (p.His1146fs) rs2054707218
NM_001113378.2(FANCI):c.3493del (p.Asp1165fs) rs758597713
NM_001113378.2(FANCI):c.3521C>T (p.Thr1174Ile) rs757106031
NM_001113378.2(FANCI):c.3604G>C (p.Gly1202Arg) rs747326740
NM_001113378.2(FANCI):c.3622_3623del (p.Leu1208fs) rs1491132258
NM_001113378.2(FANCI):c.3853C>T (p.Arg1285Ter) rs121918164
NM_001113378.2(FANCI):c.3854G>A (p.Arg1285Gln) rs121918163
NM_001113378.2(FANCI):c.3895C>T (p.Arg1299Ter) rs551305056
NM_001113378.2(FANCI):c.3901dup (p.Asp1301fs) rs2055186253
NM_001113378.2(FANCI):c.3925_*672del (p.Gly1309_Ter1329del) rs2055264556
NM_001113378.2(FANCI):c.756-25_756-19del rs2053061271
NM_001113378.2(FANCI):c.866T>C (p.Leu289Pro) rs1210148997

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